Sturge-Weber syndrome
This disease, also known as encephalotrigeminal angiomatosis, was first described by Schiremer, and later Sturge and Weber made detailed reports, hence the name Sturge-Weber syndrome. This syndrome is the only phacoma-toses without a genetic tendency, and is a developmental disease of vascular malformations of the head and face. The characteristic is that the facial area where the trigeminal nerve is distributed has capillary hemangiomas of the skin and mucosa, sometimes combined with intracranial hemangiomas or invasion of the eyes.
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Site of disease:
Eyes, skull and brain -
Infectious :
Not contagious -
Frequent population:
All groups -
Related symptoms:
visual impairment edema eye pain visual impairment edema -
Concurrent disease:
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